ENST00000405460.9:c.11503G>T
MANE Select
|
ENSP00000384582.2:p.Asp3835Tyr
|
|
ENST00000425867.3:c.634G>T
|
ENSP00000392618.3:p.Asp212Tyr
|
|
ENST00000639431.1:c.265+78899G>T
|
ENSP00000491057.1:n.265+78899G>T
|
|
ENST00000640374.1:n.4647G>T
|
|
|
ENST00000640464.1:n.1922G>T
|
|
|
ENST00000405460.6:c.11503G>T
|
ENSP00000384582.2:p.Asp3835Tyr
|
|
ENST00000509621.1:c.4200G>T
|
|
|
NM_032119.3:c.11503G>T
|
NP_115495.3:p.Asp3835Tyr
|
|
NR_003149.1:n.11516G>T
|
|
|
XM_011543675.1:c.11500G>T
|
XP_011541977.1:p.Asp3834Tyr
|
|
XM_011543676.1:c.11422G>T
|
XP_011541978.1:p.Asp3808Tyr
|
|
XM_011543677.1:c.8806G>T
|
XP_011541979.1:p.Asp2936Tyr
|
|
XM_011543678.1:c.11503G>T
|
XP_011541980.1:p.Asp3835Tyr
|
|
NM_032119.4:c.11503G>T
MANE Select
|
NP_115495.3:p.Asp3835Tyr
|
|
XM_017009963.2:c.11524G>T
|
XP_016865452.1:p.Asp3842Tyr
|
|
XM_017009964.2:c.11521G>T
|
XP_016865453.1:p.Asp3841Tyr
|
|
XM_017009965.1:c.11521G>T
|
XP_016865454.1:p.Asp3841Tyr
|
|
XM_017009966.2:c.11443G>T
|
XP_016865455.1:p.Asp3815Tyr
|
|
XM_017009967.1:c.11428G>T
|
XP_016865456.1:p.Asp3810Tyr
|
|
XM_017009968.2:c.11524G>T
|
XP_016865457.1:p.Asp3842Tyr
|
|
XM_017009969.2:c.11524G>T
|
XP_016865458.1:p.Asp3842Tyr
|
|
XM_017009970.2:c.11524G>T
|
XP_016865459.1:p.Asp3842Tyr
|
|
XM_017009971.2:c.11524G>T
|
XP_016865460.1:p.Asp3842Tyr
|
|
XM_017009972.1:c.4642G>T
|
XP_016865461.1:p.Asp1548Tyr
|
|
XM_017009973.1:c.4621G>T
|
XP_016865462.1:p.Asp1541Tyr
|
|
NR_003149.2:n.11519G>T
|
|
|